Jason Hehir
Queen Square
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
ITPR1 Deletion in a Patient With Sensory Ataxic Neuropathy and Sjögren Syndrome.
Journal: Journal of the peripheral nervous system : JPNS
Published: August 30, 2025
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's disease.
Journal: NPJ Parkinson's disease
Published: December 04, 2023
Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk.
Journal: Human molecular genetics
Published: July 15, 2020
Ambroxol for the Treatment of Patients With Parkinson Disease With and Without Glucocerebrosidase Gene Mutations: A Nonrandomized, Noncontrolled Trial.
Journal: JAMA neurology
Published: January 14, 2020
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study.
Journal: Brain : a journal of neurology
Published: September 06, 2018
Analysis of the genetic variability in Parkinson's disease from Southern Spain.
Journal: Neurobiology of aging
Published: July 23, 2015
A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations.
Journal: JAMA neurology
Published: July 09, 2014
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies.
Journal: Neurology
Published: December 24, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026